Pharma professionals looking for exciting career opportunities in Production, QA, Engineering, and Microbiology should not miss this opportunity. NATCO Pharma is conducting a Walk-In Interview on 1st March 2026 (Sunday) at Visakhapatnam, Andhra Pradesh. Candidates with experience in formulation and parenteral manufacturing are invited to attend.
This walk-in drive offers roles across multiple departments including OSD and Parenteral divisions. If you have relevant pharma manufacturing experience and are ready to work in rotational shifts, this could be your next big career move.
Interview Details
Interview Date: 1st March 2026 (Sunday)
Time: 9:00 AM to 2:00 PM
Venue: Signature Hotel, Sheelanagar (Gajuwaka), Visakhapatnam, Andhra Pradesh – 530012
Work Locations:
• Kothur (Formulation Division)
• Nagarjuna Sagar (Parenteral Division)
Departments & Open Positions
Production & Packing (OSD) – Kothur
• Operators – 5 to 8 years of experience in Granulation, Compression, Coating, Capsule Filling, Bottle/Blister Packing, IPQC, Labelling & Printing
• Executives – 4 to 8 years of experience in supervising Production activities
• Executive/Sr Executive (QMS) – 4 to 8 years of experience in Change Control, Investigations, Incidents & CAPA
Production – Parenteral Division
• Assistant Manager – 12+ years of sterile injectable manufacturing experience
• Filling Supervisors – 2 to 3 years of aseptic filling experience
• Packing Supervisor – B.Pharm (Fresher)
• General Injectables Packing In-charge – 12+ years of experience
• QMS Executive – 3+ years of QMS, GMP & SOP knowledge
• Training Supervisor – B.Pharm (Fresher)
• Operators – 2 to 3 years in Filling, Compounding, Autoclave operations
Engineering
• Lyo In-charge – 8 to 10 years of lyophilization experience
• Instrumentation Expert – 4 to 6 years of experience
Microbiology
• Disinfectant & Media Preparation
• MLT, BET & Sterility Validation Execution
• 2 to 6 years of experience required
Qualification: M.Sc (Microbiology/Biotechnology)
Quality Assurance
• IPQA – 3 to 5 years
• Documentation – 3 to 5 years
• Documentation In-charge – 10 to 12 years
• Document Review – 5 to 8 years
• QMS – 3 to 5 years
• Vendor Management – 3 to 5 years
• Validation – 6 to 8 years
• Assistant Manager (IPQA, Validation & QMS) – 12 to 18 years
Required Qualifications
• ITI / Diploma
• B.Sc / B.Tech
• B.Pharm / M.Pharm
• M.Sc (Microbiology/Biotechnology)
Candidates must have relevant formulation or parenteral experience. Only candidates with regulatory exposure will be considered. Willingness to work in rotational and night shifts is mandatory.
Roles & Responsibilities
• Handling manufacturing and packing operations as per GMP guidelines
• Ensuring compliance with cGMP, SOPs, and regulatory standards
• Managing documentation, QMS, validation, and CAPA activities
• Supervising production teams and ensuring productivity targets
• Executing sterile injectable and OSD manufacturing processes
• Supporting audits, investigations, and quality improvements
Salary & Benefits
Estimated Salary Range: INR 1.8 LPA to 12 LPA (based on role and experience)
Benefits may include:
• Performance-based increments
• Exposure to regulatory manufacturing
• Career growth opportunities
• Learning & development programs
• Health and statutory benefits as per company policy
How to Apply
Eligible candidates can directly attend the walk-in interview at the given venue on 1st March 2026 with:
• Updated Resume
• Educational Certificates
• Experience Certificates
• Latest Salary Slip
• Government ID Proof
Early arrival is recommended to avoid last-minute rush.
Important Note
• Candidates must be open to rotational shifts including night shifts
• Preference may be given to candidates with relevant formulation exposure
• Only relevant and eligible profiles will be shortlisted
This is an excellent opportunity for pharma professionals seeking career growth in a reputed pharmaceutical manufacturing setup.
